Canonical Allele Identifier: CA1854131349

Gene: TJP2

Linked Data

• dbSNP Id: rs1830949892
• gnomAD v4: 9-69246666-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69246668del , CM000671.2:g.69246668del	GRCh38
NC_000009.11:g.71861584del , CM000671.1:g.71861584del	GRCh37
NC_000009.10:g.71051404del	NCBI36
NG_016342.1:g.130361del
NG_016342.2:g.150762del

Transcript Alleles

HGVS	Amino-acid change
ENST00000348208.9:c.2567-22del	ENSP00000345893.4:n.2567-22del
ENST00000377245.9:c.2567-22del MANE Select	ENSP00000366453.4:n.2567-22del
ENST00000498204.2:n.1982del
ENST00000535702.6:c.2579-22del	ENSP00000442090.1:n.2579-22del
ENST00000539225.2:c.2660-22del	ENSP00000438262.1:n.2660-22del
ENST00000636247.1:n.2646-22del
ENST00000636438.1:c.2744-22del	ENSP00000489860.1:n.2744-22del
ENST00000642889.1:c.2954-22del	ENSP00000493780.1:n.2954-22del
ENST00000643352.1:c.*2755-22del	ENSP00000496488.1:n.*2755-22del
ENST00000645088.1:c.*2874-22del	ENSP00000495447.1:n.*2874-22del
ENST00000647986.1:c.2498-22del	ENSP00000496877.1:n.2498-22del
ENST00000648042.1:c.1276-22del
ENST00000648087.1:n.2877-22del
ENST00000649114.1:c.2567-22del	ENSP00000497328.1:n.2567-22del
ENST00000649134.1:c.2579-22del	ENSP00000498068.1:n.2579-22del
ENST00000649783.1:n.2591-22del
ENST00000649927.1:n.112-22del
ENST00000649943.1:c.2567-22del	ENSP00000497539.1:n.2567-22del
ENST00000650084.1:c.2570-22del	ENSP00000497861.1:n.2570-22del
ENST00000650333.1:c.2498-22del	ENSP00000496791.1:n.2498-22del
ENST00000650460.1:c.1840-6147del
ENST00000650522.1:n.2090-22del
ENST00000265384.11:c.2567-22del	ENSP00000265384.7:n.2567-22del
ENST00000348208.8:c.2567-22del	ENSP00000345893.4:n.2567-22del
ENST00000377245.8:c.2567-22del	ENSP00000366453.4:n.2567-22del
ENST00000453658.6:c.2498-22del	ENSP00000392178.2:n.2498-22del
ENST00000498204.1:n.443del
ENST00000535702.5:c.2579-22del	ENSP00000442090.1:n.2579-22del
ENST00000539225.1:c.2660-22del	ENSP00000438262.1:n.2660-22del
NM_001170414.2:c.2498-22del	NP_001163885.1:n.2498-22del
NM_001170415.1:c.2579-22del	NP_001163886.1:n.2579-22del
NM_001170416.1:c.2660-22del	NP_001163887.1:n.2660-22del
NM_001170630.1:c.2567-22del	NP_001164101.1:n.2567-22del
NM_004817.3:c.2567-22del	NP_004808.2:n.2567-22del
NM_201629.3:c.2567-22del	NP_963923.1:n.2567-22del
XM_005252314.1:c.2579-22del	XP_005252371.1:n.2579-22del
XM_006717324.2:c.2561-22del	XP_006717387.1:n.2561-22del
XM_011519204.1:c.2498-22del	XP_011517506.1:n.2498-22del
XM_011519205.1:c.2498-22del	XP_011517507.1:n.2498-22del
XM_011519206.1:c.2498-22del	XP_011517508.1:n.2498-22del
XM_011519207.1:c.2498-22del	XP_011517509.1:n.2498-22del
XM_011519208.1:c.2498-22del	XP_011517510.1:n.2498-22del
XM_011519209.1:c.2498-22del	XP_011517511.1:n.2498-22del
NM_004817.4:c.2567-22del MANE Select	NP_004808.2:n.2567-22del
XM_005252314.2:c.2579-22del	XP_005252371.1:n.2579-22del
XM_011519206.2:c.2498-22del	XP_011517508.1:n.2498-22del
XM_011519207.2:c.2498-22del	XP_011517509.1:n.2498-22del
XM_011519208.2:c.2498-22del	XP_011517510.1:n.2498-22del
XM_011519209.2:c.2498-22del	XP_011517511.1:n.2498-22del
XM_017015327.2:c.2567-22del	XP_016870816.1:n.2567-22del
XM_017015328.1:c.2579-22del	XP_016870817.1:n.2579-22del
NM_001170416.2:c.2660-22del	NP_001163887.1:n.2660-22del
NM_001369870.1:c.2492-22del	NP_001356799.1:n.2492-22del
NM_001369871.1:c.2498-22del	NP_001356800.1:n.2498-22del
NM_001369872.1:c.2567-22del	NP_001356801.1:n.2567-22del
NM_001369873.1:c.2567-22del	NP_001356802.1:n.2567-22del
NM_001369874.1:c.2579-22del	NP_001356803.1:n.2579-22del
NM_001369875.1:c.2579-22del	NP_001356804.1:n.2579-22del